Canonical Allele Identifier: PA2826961667
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 861095
ClinVar RCV Id: RCV001067535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304113.1:p.Thr478Ser
CA396465074
NM_001317184.2:c.1432A>T
CA396465079
NM_001317184.2:c.1433C>G